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Pathophysiology and treatment of patients with beta-thalassemia – an update
Thalassemia (thal) is an autosomal recessive, hereditary, chronic hemolytic anemia due to a partial or complete deficiency in the synthesis of α-globin chains (α-thal) or β-globin chains (β-thal) that compose the major adult hemoglobin (α (2)β (2).) It is caused by one or more mutations in the corre...
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| Publicado en: | F1000Res |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
F1000 Research Limited
2017
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5749127/ https://ncbi.nlm.nih.gov/pubmed/29333256 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.12688/f1000research.12688.1 |
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